首页 | 本学科首页   官方微博 | 高级检索  
     检索      

新兽药盐酸沃尼妙林的合成
引用本文:薛克友.新兽药盐酸沃尼妙林的合成[J].中国兽药杂志,2014,48(10):22-25.
作者姓名:薛克友
作者单位:武汉回盛生物科技有限公司,湖北省兽药工程技术研究中心,武汉430042
摘    要:以精制的截短侧耳素为原料,经对甲苯磺酰氯磺化后,与二甲基半胱胺盐酸盐反应,制得截短侧耳素半胱胺取代物;另外由D-缬氨酸、乙酰乙酸甲酯和氢氧化钾反应制得( R)-2-(1-甲氧羰基-2-烯丙基)氨基-3-甲基丁酸钾,经氯甲酸乙酯活化后与截短侧耳素半胱胺取代物反应,最后通过调节pH值,经反相萃取后,冻干得盐酸沃尼妙林,总收率为69%,所得产品按照EP6.0进行了质量检测,产品具有含量高、杂质少等优点。

关 键 词:盐酸沃尼妙林  合成  截短侧耳素
收稿时间:2014/7/14 0:00:00
修稿时间:2014/9/11 0:00:00

The Synthesis of New Veterinary Drug Valnemulin hydrochloride
XUE Ke-you , GE Jian , SHEN Hua , ZHANG Wei-yuan , LIU Jie.The Synthesis of New Veterinary Drug Valnemulin hydrochloride[J].Chinese Journal of Veterinary Drug,2014,48(10):22-25.
Authors:XUE Ke-you  GE Jian  SHEN Hua  ZHANG Wei-yuan  LIU Jie
Institution:Wuhan Hvsen Biotechnology Co., Ltd., Hubei Province Veterinary Drug Engineering Research Center
Abstract:Pleuromutilin refined as raw material and reacted with the sulfonated toluene sulfonyl chloride, dimethyl cysteamine hydrochloride to prepare cysteamine substituent; D-valine and methyl acetoacetate were reacted with potassium to obtain (R)-2-(1-methoxycarbonyl-2-allyl)amino-3-methylbut-potassium, follow by activated with ethyl chloroformate to react with pleuromutilin cysteamine substitution, and finally by adjusting the pH and inverting extraction to obtain valnemulin hydrochloride with the total yield of 69%. The product was tested according with EP6.0 to have high content and low impurities and so on.
Keywords:hydrochloride Valnemulin  synthesis study  Pleuromutilin
本文献已被 维普 等数据库收录!
点击此处可从《中国兽药杂志》浏览原始摘要信息
点击此处可从《中国兽药杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号